Variant #0000729365 (NC_000001.10:g.94487490A>G, NM_000350.2:c.4685T>C (ABCA4))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.94487490A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABCA4_000506 See all 80 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1762111
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00122 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-02-10 14:48:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCA4 NM_000350.2 ?/. - c.4685T>C r.(?) p.(Ile1562Thr)


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